Related Experiment Video
Updated: May 16, 2026

HPLC Coupled with Chemical Fingerprinting for Multi-Pattern Recognition for Identifying the Authenticity of Clematidis Armandii Caulis
Published on: November 11, 2022
[Determination of carboxyatractyloside and atractyloside in Xanthii Fructus by HPLC]
Rui Duo1, Yan Chen, Yuhong Liu
1Sichuan Academy of Chinese Medicine Sciences, Chengdu 610041, China. 165185553@qq.com
Objective:
To determine carboxyatractyloside and atractyloside in Xanthii Fructus by HPLC.
Method:
By HPLC, Agilent ZORBAX SB-phenyl (4.6 mm x 250 mm, 5 microm) column was adopted, with acetonitrile-0.01 mol x L(-1) NaH2PO4 (pH 6) as the mobile phase for gradient elution at the flow rate of 1.0 mL x min(-1). The detection wavelength was 203 nm, and the temperature was set at 35 degrees C.
Result:
Carboxyatractyloside showed a good linearity within the range of 0.0972-1.944 microg and atractyloside showed a good linearity within the range of 0.1030-2.060 microg. The recovery rate of carboxyatractyloside was 100. 3% and that of atractyloside was 102.5%. The RSD were 0.67% and 1.4% (n=6).
Conclusion:
This method is so simple, practical and highly repeatable that is can be used for quality control of Xanthii Fructus.
